Canonical Allele Identifier: CA2637632298

Gene: TCAP

Linked Data

• gnomAD v4: 17-39665581-A-AAT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665582_39665583dup , CM000679.2:g.39665582_39665583dup	GRCh38
NC_000017.10:g.37821835_37821836dup , CM000679.1:g.37821835_37821836dup	GRCh37
NC_000017.9:g.35075361_35075362dup	NCBI36
NG_008892.1:g.5237_5238dup , LRG_210:g.5237_5238dup
NG_042278.1:g.2602_2603dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.110+113_110+114dup MANE Select	ENSP00000312624.2:n.110+113_110+114dup
ENST00000309889.2:c.110+113_110+114dup	ENSP00000312624.2:n.110+113_110+114dup
ENST00000578283.1:c.110+113_110+114dup	ENSP00000462787.1:n.110+113_110+114dup
NM_003673.3:c.110+113_110+114dup , LRG_210t1:c.110+113_110+114dup	NP_003664.1:n.110+113_110+114dup
NM_003673.4:c.110+113_110+114dup MANE Select	NP_003664.1:n.110+113_110+114dup